Gene-specific Copy Number Variation Probe-NRXN1
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| Catalog: |
CNVFP-NRXN1-14396 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NRXN1). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
NRXN1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NRXN1 genes. This product achieves the purpose of detection by hybridizing with the NRXN1 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
Neurexin 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a single-pass type I membrane protein that belongs to the neurexin family. Neurexins are cell-surface receptors that bind neuroligins to form Ca(2+)-dependent neurexin/neuroligin complexes at synapses in the central nervous system. This complex is required for efficient neurotransmission and is involved in the formation of synaptic contacts. Three members of this gene family have been studied in detail and are estimated to generate over 3,000 variants through the use of two alternative promoters (alpha and beta) and extensive alternative splicing in each family member. Recently, a third promoter (gamma) was identified for this gene in the 3' region. Mutations in this gene are associated with Pitt-Hopkins-like syndrome-2 and may contribute to susceptibility to schizophrenia. [provided by RefSeq, Aug 2016] |
| Gene Symbol |
NRXN1 |
| Location |
2p16.3 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 50145642-51259674 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-NRXN1-14396-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NRXN1-14396-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NRXN1-14396-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NRXN1-14396-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NRXN1-14396-AQ |
467nm |
418nm |
|
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